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DNA Labs India

Chromosome Analysis (Karyotype) Blood Test

DNA Labs India | ISO 9001:2015 Certified

Chromosome Analysis (Karyotype) Blood Test

Also known as: Karyotype Analysis, Chromosomal Analysis

Chromosome Analysis (Karyotype) Blood Test test available at DNA Labs India for ₹4,000. Uses Culture, Robotic Microscopy, Karyotype on Blood samples. Results in 10-12 working days. Free home collection in 300+ cities across India.

Blood TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of chromosome analysis is to identify chromosomal abnormalities or disorders, such as aneuploidies, translocations, deletions, or duplications, which can cause genetic conditions, birth defects, or developmental delays.

Test Code
304
Price
₹4,000
Sample Type
Blood
Result Time
10-12 working days
Fasting Required
No
Method
Culture, Robotic Microscopy, Karyotype
Step 1

Sample Collection

Duly filled Chromosome & FISH Analysis Requisition form (Form 17) is mandatory.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample is collected via venipuncture from a vein in the arm.

Step 3

Report Delivery

Apply pressure to the collection site to prevent bruising. No specific restrictions post-collection.

Timeline: 10-12 working days

Patient Instructions

1
Before the Test:Complete the required requisition form and inform the healthcare provider of any medications or conditions.
2
During the Test:The test involves a standard blood draw; the sample is then processed in the lab for chromosome culture and analysis.
3
After the Test:No special care is needed; await results and follow up with your doctor.

About This Test

Who Should Get This Test

The purpose of chromosome analysis is to identify chromosomal abnormalities or disorders, such as aneuploidies, translocations, deletions, or duplications, which can cause genetic conditions, birth defects, or developmental delays.

How to Prepare

  • Complete Form 17 prior to sample collection
  • Ensure sample is transported at room temperature

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"This test is crucial for diagnosing chromosomal abnormalities in patients with developmental delays, recurrent miscarriages, or infertility, aiding in informed clinical decisions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood
ContainerSodium Heparin
Collection MethodVenipuncture

Sample Stability

Room Temperature
Refrigerator
Frozen
Sample Rejection Criteria:
  • Hemolyzed or clotted sample
  • Improperly labeled specimen
  • Insufficient sample volume

Understanding Your Results

Results from chromosome analysis are interpreted by comparing the observed karyotype to normal chromosomal patterns. Abnormalities may indicate genetic disorders.
📊

Normal Karyotype

No chromosomal abnormalities detected.

📊

Aneuploidy (e.g., Trisomy 21)

Presence of extra or missing chromosomes, associated with conditions like Down syndrome.

📊

Structural Abnormality (e.g., Translocation)

Changes in chromosome structure, which may be balanced or unbalanced.

📊

Mosaicism

Presence of two or more cell lines with different karyotypes.

⚠️ When to Consult a Doctor:

Consult a healthcare provider if results indicate abnormalities, or if symptoms such as developmental delays, recurrent miscarriages, or infertility persist.

Limitations

  • Cannot detect small genetic mutations
  • Requires viable cells for culture
  • Longer turnaround time compared to some molecular tests

Risks & Considerations

  • Bruising at the collection site
  • Infection (rare)
  • Fainting or dizziness during blood draw

Interfering Factors

  • Contaminated sample
  • Improper handling or storage
  • Cell culture failure

Frequently Asked Questions

What is a Chromosome Analysis (Karyotype) test?
It is a blood test that examines the structure and number of chromosomes in cells to diagnose genetic disorders.
Why is this test recommended?
It is recommended for symptoms like developmental delays, infertility, recurrent miscarriages, or suspicion of genetic disorders such as Down syndrome.
How is the test performed?
A blood sample is collected, white blood cells are cultured, chromosomes are harvested, stained, and examined under a microscope.
What does the test detect?
It detects chromosomal abnormalities like aneuploidies (e.g., trisomy), translocations, deletions, and duplications.
Is fasting required for this test?
No, fasting is not required, but a duly filled requisition form is mandatory.
How long does it take to get results?
Results are typically available in 10-12 working days.
What are the risks of this test?
Risks are minimal and include bruising at the blood draw site and rare infection.
Can this test be done during pregnancy?
Yes, it can be used for prenatal diagnosis, often via amniocentesis or chorionic villus sampling, but for blood tests, consult your healthcare provider.
What is the cost of the test?
The cost at DNA Labs India is INR 4000, with free home sample collection available across India.
Is home collection available?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities.
What should I do if my results are abnormal?
Consult your healthcare provider or a genetic counselor for further evaluation and management options.
How accurate is chromosome analysis?
It is highly accurate for detecting large chromosomal abnormalities but may not detect small genetic mutations.
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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