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Chromosome Analysis Philadelphia Test

DNA Labs India | ISO 9001:2015 Certified

Chromosome Analysis Philadelphia Test

Short Name: Philadelphia Chromosome Test

Also known as: Philadelphia Chromosome Analysis, Ph Chromosome Test, Karyotyping for Philadelphia Chromosome

Chromosome Analysis Philadelphia Test test available at DNA Labs India for ₹4,000. Uses Cell Culture, Microscopy, Karyotyping on Bone marrow aspirate (1.5 mL min.) samples. Results in 7 working days. Free home collection in 300+ cities across India.

Cytogenetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The primary purpose of the Chromosome Analysis Philadelphia Test is to identify the presence of the Philadelphia chromosome, which is crucial for diagnosing chronic myeloid leukemia (CML) and other related hematological disorders. It helps in confirming genetic abnormalities that may cause symptoms like developmental delays or infertility, enabling targeted treatment and genetic counseling.

Test Code
310
Price
₹4,000
Sample Type
Bone marrow aspirate (1.5 mL min.)
Result Time
7 working days
Fasting Required
No
Method
Cell Culture, Microscopy, Karyotyping
Step 1

Sample Collection

Duly filled Chromosome & FISH Analysis Requisition form (Form 17) is mandatory. Ensure sample collection is scheduled appropriately.

Method: Bone marrow aspiration

Step 2

Laboratory Analysis

Bone marrow aspiration performed by a healthcare professional using a heparinized tube.

Step 3

Report Delivery

Sample must be refrigerated immediately and shipped to the lab within 24 hours. Do not freeze.

Timeline: 7 working days

Patient Instructions

1
Before the Test:Complete the Chromosome & FISH Analysis Requisition form (Form 17). No fasting is required, but follow any specific instructions from your healthcare provider.
2
During the Test:The test involves culturing bone marrow cells, followed by microscopic examination and karyotyping to analyze chromosomes.
3
After the Test:Results are typically available within 7 working days and can be accessed online or through your healthcare provider.

About This Test

Who Should Get This Test

The primary purpose of the Chromosome Analysis Philadelphia Test is to identify the presence of the Philadelphia chromosome, which is crucial for diagnosing chronic myeloid leukemia (CML) and other related hematological disorders. It helps in confirming genetic abnormalities that may cause symptoms like developmental delays or infertility, enabling targeted treatment and genetic counseling.

How to Prepare

  • Collect bone marrow sample in Sodium Heparin tube.
  • Ship refrigerated immediately.
  • Do not freeze the sample.
  • Include completed requisition form (Form 17).
  • Ensure sample reaches the lab within 24 hours.

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"This test is crucial for diagnosing chromosomal abnormalities, including Philadelphia chromosome in chronic myeloid leukemia, and should be considered for patients with symptoms like unexplained fatigue, weight loss, or recurrent infections."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBone marrow aspirate (1.5 mL min.)
Sample Volume1.5 mL min.
Container1 Green Top (Sodium Heparin) tube
Collection MethodBone marrow aspiration

Sample Stability

Room Temperature
Refrigerator
Frozen
Sample Rejection Criteria:
  • Sample frozen or not refrigerated
  • Insufficient sample volume (less than 1.5 mL)
  • Missing or incomplete requisition form
  • Sample received after 24 hours of collection

Understanding Your Results

Results from the Chromosome Analysis Philadelphia Test are interpreted based on the presence or absence of chromosomal abnormalities. A positive result indicates the detection of the Philadelphia chromosome, which is associated with chronic myeloid leukemia (CML), while a negative result suggests normal chromosomes or absence of the specific translocation.
📊

Positive for Philadelphia chromosome

Presence of t(9;22)(q34;q11.2) translocation, indicative of CML or related disorders. Further clinical evaluation and treatment planning are recommended.

📊

Normal karyotype

No chromosomal abnormalities detected, including absence of Philadelphia chromosome. Clinical correlation is advised if symptoms persist.

📊

Other chromosomal abnormalities

Detection of non-Philadelphia abnormalities, which may indicate different genetic conditions. Consult a geneticist for detailed analysis.

⚠️ When to Consult a Doctor:

Consult your doctor if you experience symptoms such as unexplained fatigue, weight loss, night sweats, recurrent infections, or if you have a family history of genetic disorders. Early diagnosis can improve management outcomes.

Limitations

  • May not detect all chromosomal abnormalities
  • Requires viable cells for accurate analysis
  • Cannot identify gene-level mutations without additional tests like FISH

Risks & Considerations

  • Minimal risks from bone marrow aspiration, such as bruising, infection, or discomfort at the collection site.

Interfering Factors

  • Improper sample storage (e.g., freezing)
  • Delayed sample processing beyond 24 hours
  • Contaminated or insufficient sample volume

Compare With Similar Tests

TestChromosome Analysis Philadelphia TestFISH for BCR-ABL1KaryotypingBone Marrow BiopsyComplete Blood Count (CBC)
ComparisonChromosome Analysis Philadelphia TestMore specific for Philadelphia chromosome detection using fluorescent probes, often used as a confirmatory test.Standard method for chromosome analysis, provides a comprehensive view of chromosomal structure and number.Invasive procedure to examine bone marrow cells, often combined with chromosome analysis for hematological disorders.Routine blood test that may show abnormalities suggestive of leukemia but does not detect specific chromosomal changes.

Frequently Asked Questions

What is the Chromosome Analysis Philadelphia Test?
It is a diagnostic test that examines chromosomes in bone marrow cells to detect the Philadelphia chromosome, associated with chronic myeloid leukemia (CML) and other genetic disorders.
Why is this test recommended?
It is recommended for individuals with symptoms such as developmental delays, intellectual disability, birth defects, infertility, recurrent miscarriage, or suspected cancer like CML.
What is the cost of the test?
The cost at DNA Labs India is INR 4000, which includes home sample collection and report delivery.
How is the sample collected?
A bone marrow aspirate is collected in a Sodium Heparin tube by a healthcare professional and shipped refrigerated to the lab.
Is fasting required for this test?
No, fasting is not required for the Chromosome Analysis Philadelphia Test.
How long does it take to get the report?
Results are typically available within 7 working days after sample receipt at the laboratory.
What does a positive result mean?
A positive result indicates the presence of the Philadelphia chromosome, suggesting chronic myeloid leukemia (CML) or related conditions. Further medical consultation is advised.
Are there any risks associated with the test?
Risks are minimal and may include bruising or discomfort at the bone marrow aspiration site. Infection risk is low with proper procedure.
How should I prepare for the test?
Ensure the requisition form (Form 17) is completed and available. No special preparation is needed otherwise.
Is the test covered by insurance?
Coverage varies by insurance plan. Check with your provider to see if the test is covered under your policy.
Can the test be done at home?
Yes, DNA Labs India offers free home sample collection for this test across many cities in India.
What are the limitations of the test?
Limitations include inability to detect all chromosomal abnormalities and reliance on viable cells. Additional tests like FISH may be needed for comprehensive analysis.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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