Skip to main content
DNA Labs India

Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test

DNA Labs India | ISO 9001:2015 Certified

Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test

Short Name: CLL Mutations Panel 1

Also known as: CLL Genetic Panel, CLL Mutations Panel

Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test test available at DNA Labs India for ₹5,000. Uses PCR - MLPA on Whole blood samples. Results in Reports available by Saturday if sample received by Monday 11 am.. Free home collection in 300+ cities across India.

Genetic TestAdults🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr Pasupathy Arumugam

Dr Pasupathy Arumugam

Consultant Pathologist · Reg: 21521

Last reviewed: September 7, 2026

Overview

The purpose of the CLL Mutations Detection Panel 1 Test is to detect genetic mutations and chromosomal abnormalities in Chronic Lymphocytic Leukemia cells, which includes: Chromosome 2p gain, 6q deletion, 8p loss & 8q amplification, 9p21 loss, 11q deletion, Trisomy 12, 13q14 deletion, and 17p deletion. These findings help in prognosis, risk stratification, and guiding targeted therapy.

Test Code
319
Price
₹5,000
Sample Type
Whole blood
Result Time
Reports available by Saturday if sample received by Monday 11 am.
Fasting Required
No
Method
PCR - MLPA
Step 1

Sample Collection

Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Method: Venipuncture

Step 2

Laboratory Analysis

Standard venipuncture procedure using Lavender top (EDTA) tube.

Step 3

Report Delivery

Ship refrigerated. DO NOT FREEZE. Ensure sample is labeled correctly.

Timeline: Reports available by Saturday if sample received by Monday 11 am.

Patient Instructions

1
Before the Test:Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
2
During the Test:Blood sample is collected and processed using PCR - MLPA method.
3
After the Test:Results are reviewed by a specialist and reported online.

About This Test

Who Should Get This Test

The purpose of the CLL Mutations Detection Panel 1 Test is to detect genetic mutations and chromosomal abnormalities in Chronic Lymphocytic Leukemia cells, which includes: Chromosome 2p gain, 6q deletion, 8p loss & 8q amplification, 9p21 loss, 11q deletion, Trisomy 12, 13q14 deletion, and 17p deletion. These findings help in prognosis, risk stratification, and guiding targeted therapy.

How to Prepare

  • Collect 4 mL whole blood in Lavender top (EDTA) tube
  • Mix gently to avoid clotting
  • Ship refrigerated within 6 hours at room temperature or 72 hours in refrigerator
  • Do not freeze the sample

Doctor's Notes

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

"This test is crucial for identifying genetic mutations in CLL, which can guide targeted therapy and improve patient outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Room Temperature: 6 hours
Refrigerator: 72 hours
Frozen: Not applicable
Sample Rejection Criteria:
  • Sample hemolyzed or clotted
  • Insufficient volume
  • Improper labeling or missing requisition form

Understanding Your Results

Results indicate the presence or absence of specific genetic mutations associated with CLL. Positive results may suggest a more aggressive form or guide treatment options.
📊

Associated with poor prognosis and resistance to certain chemotherapies

📊

May indicate higher risk and need for targeted therapy

📊

Often linked to intermediate prognosis

📊

Generally associated with better prognosis when isolated

⚠️ When to Consult a Doctor:

If symptoms persist or worsen, or if test results indicate mutations requiring specialized treatment.

Limitations

  • ⚠May not detect all genetic mutations
  • ⚠Results should be interpreted in conjunction with clinical findings
  • ⚠Not a standalone diagnostic tool

Risks & Considerations

  • ●Minimal risk from blood draw: bruising, infection, or dizziness

Interfering Factors

  • ●Improper sample handling or storage
  • ●Contamination during DNA extraction
  • ●Low sample volume

Compare With Similar Tests

TestChronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 TestComplete Blood Count (CBC)Flow Cytometry
ComparisonChronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test

Frequently Asked Questions

What is the CLL Mutations Detection Panel 1 Test?
It is a genetic test that detects specific mutations in Chronic Lymphocytic Leukemia cells to aid in diagnosis and treatment planning.
Why is this test recommended?
It is recommended for patients with suspected or diagnosed CLL to identify genetic mutations that influence prognosis and therapy choices.
How is the test performed?
A blood sample is collected and analyzed using PCR - MLPA to detect chromosomal abnormalities.
What mutations does the test detect?
It detects mutations such as TP53, SF3B1, ATM, NOTCH1, and chromosomal changes like 17p deletion, 11q deletion, trisomy 12, etc.
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 within 5-6 days after sample collection.
What is the cost of the test?
The test costs INR 5000.0 in India, with home sample collection available.
Is home collection available?
Yes, free home sample collection is available for online bookings across many cities in India.
What do the results mean?
Results indicate the presence of genetic mutations, which help in assessing disease risk and guiding treatment.
Are there any risks associated with the test?
The test involves a standard blood draw with minimal risks like bruising or infection.
Can this test be used for treatment planning?
Yes, identifying mutations can help doctors choose targeted therapies for better outcomes.
How often should this test be repeated?
It is usually done once for initial diagnosis, but repeat testing may be needed based on disease progression or treatment response.
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.

Related Tests

B-Cell Rearrangement Detection Test

₹22,000

Acute Lymphoblastic Leukemia (ALL) Cytogenetics Panel Test

₹20,000

Epstein-Barr Virus Early RNA (EBER-ISH) In-Situ-Hybridization Test

₹6,000

OncoPro NCCN Lung Cancer Panel with PD-L1 Test

₹140,400

Acute Myeloid Leukemia (AML) Cytogenetics Panel Test

₹23,000

AML ETO t(8;21) Gene Rearrangement PCR Qualitative Test

₹6,000
For Hospitals & Clinics

Reference Laboratory Services

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.

LIMS Integration

Your Data Privacy

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.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.