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DNA Labs India

Chronic Lymphocytic Leukemia (CLL) Mutations Detection Comprehensive Panel Test

DNA Labs India | ISO 9001:2015 Certified

Chronic Lymphocytic Leukemia (CLL) Mutations Detection Comprehensive Panel Test

Short Name: CLL Mutations Comprehensive Panel

Also known as: CLL Panel Test, Leukemia Mutation Detection Panel, CLL Genetic Test

Chronic Lymphocytic Leukemia (CLL) Mutations Detection Comprehensive Panel Test test available at DNA Labs India for ₹9,000. Uses PCR - MLPA on Whole blood samples. Results in Sample accepted Monday by 11 AM; reports available by Saturday.. Free home collection in 300+ cities across India.

OncologistAdults🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect specific genetic mutations and chromosomal abnormalities in Chronic Lymphocytic Leukemia patients for prognosis assessment, treatment planning, and monitoring disease progression.

Test Code
318
Price
₹9,000
Sample Type
Whole blood
Result Time
Sample accepted Monday by 11 AM; reports available by Saturday.
Fasting Required
No
Method
PCR - MLPA
Step 1

Sample Collection

Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory. No fasting required.

Method: Venipuncture

Step 2

Laboratory Analysis

A small blood sample is collected via venipuncture into an EDTA tube.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding. Resume normal activities.

Timeline: Sample accepted Monday by 11 AM; reports available by Saturday.

Patient Instructions

1
Before the Test:Complete the Genomics Clinical Information Requisition Form (Form 20) and ensure no special preparation is needed.
2
During the Test:Blood sample collection via venipuncture; process takes a few minutes.
3
After the Test:No restrictions; monitor the puncture site for any issues.

About This Test

Who Should Get This Test

To detect specific genetic mutations and chromosomal abnormalities in Chronic Lymphocytic Leukemia patients for prognosis assessment, treatment planning, and monitoring disease progression.

How to Prepare

  • Use 1 Lavender top (EDTA) tube for 4 mL whole blood
  • Ship sample refrigerated; do not freeze
  • Ensure the Genomics Clinical Information Requisition Form (Form 20) is fully completed
  • Maintain sample stability as per guidelines

Doctor's Notes

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

"This panel identifies key genetic mutations in CLL to guide targeted therapies and improve treatment outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeWhole blood
Sample Volume4 mL (2 mL min.)
Container1 Lavender top (EDTA) tube
Collection MethodVenipuncture

Sample Stability

Room Temperature: 6 hours
Refrigerator: 72 hours
Frozen: Not acceptable
Sample Rejection Criteria:
  • Hemolyzed or clotted sample
  • Incorrect sample container
  • Missing or incomplete requisition form
  • Sample stored beyond stability limits

Understanding Your Results

Results indicate the presence or absence of specific genetic mutations and chromosomal abnormalities. Detection may inform prognosis, guide treatment selection, and assess risk levels.
Positive result for mutations may indicate higher risk or need for targeted therapy
Negative result suggests absence of detected mutations, but clinical correlation is essential
Chromosomal abnormalities like deletions or gains can impact treatment decisions
Consult with an oncologist for comprehensive interpretation and next steps
⚠️ When to Consult a Doctor:

Consult your oncologist if you experience symptoms of CLL, require interpretation of test results, or need guidance on treatment options based on genetic findings.

Limitations

  • May not detect all possible mutations in CLL
  • Results should be interpreted alongside clinical and other diagnostic findings
  • Not intended for prenatal or predictive testing
  • Sensitivity may vary based on sample quality

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or soreness
  • Rare chance of infection at puncture site
  • No significant risks associated with genetic analysis

Interfering Factors

  • Sample hemolysis
  • Improper sample storage or handling
  • Recent blood transfusion affecting DNA quality
  • Contamination during sample collection

Compare With Similar Tests

TestChronic Lymphocytic Leukemia (CLL) Mutations Detection Comprehensive Panel TestFISH for CLLKaryotypingNext-Generation Sequencing (NGS)Flow Cytometry
ComparisonChronic Lymphocytic Leukemia (CLL) Mutations Detection Comprehensive Panel TestFISH detects specific chromosomal abnormalities but is less comprehensive for point mutations.Karyotyping provides overall chromosomal view but lacks sensitivity for small mutations.NGS offers broader genetic profiling but may be more costly and time-consuming.Flow cytometry analyzes cell surface markers but does not detect genetic mutations.

Frequently Asked Questions

What is the CLL Mutations Detection Comprehensive Panel Test?
It is a genetic test that analyzes DNA from blood samples to detect mutations and chromosomal abnormalities associated with Chronic Lymphocytic Leukemia, aiding in personalized treatment planning.
How much does the test cost at DNA Labs India?
The test costs INR 9000.0, which includes home sample collection across India.
What sample is required for the test?
A 4 mL whole blood sample collected in an EDTA tube is required. The minimum volume is 2 mL.
Is fasting required before the test?
No, fasting is not required. However, a duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
How is the test performed?
The test uses PCR-MLPA technology to analyze DNA for specific mutations and deletions relevant to CLL.
What mutations does the test detect?
It detects mutations such as SF3B1 K700E, MYD88 L265P, NOTCH1 p.2514 fs, and chromosomal abnormalities like 17p deletion and trisomy 12.
Who should consider this test?
Individuals with symptoms of CLL, confirmed diagnosis, or those seeking genetic profiling for treatment decisions should consider this test.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across many cities in India.
How long does it take to get results?
Results are typically available within 5-7 days, with samples accepted Monday by 11 AM and reports by Saturday.
Is the test covered by insurance?
Yes, the test is covered by most insurance plans. Financial assistance may be available for eligible individuals.
What do the results mean?
Results indicate the presence or absence of genetic mutations, which help in prognosis and treatment planning. Interpretation should be done by a qualified oncologist.
Are there any risks associated with the test?
The risks are minimal, similar to a standard blood draw, such as bruising or soreness at the puncture site.
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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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

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Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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