Skip to main content
DNA Labs India

FISH - 22q Deletion or LSI Di George / VCFS Test

DNA Labs India | ISO 9001:2015 Certified

FISH - 22q Deletion or LSI Di George / VCFS Test

Also known as: DiGeorge Syndrome, VCFS, 22q11.2 Deletion Syndrome, DiGeorge/VCFS Syndrome

FISH - 22q Deletion or LSI Di George / VCFS Test test available at DNA Labs India for ₹8,000. Uses FISH on Whole blood samples. Results in 4 Working days. Free home collection in 300+ cities across India.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose genetic disorders related to 22q11.2 deletion, such as DiGeorge syndrome and VCFS, enabling timely management and genetic counseling.

Test Code
565
Price
₹8,000
Sample Type
Whole blood
Result Time
4 Working days
Fasting Required
No
Method
FISH
Step 1

Sample Collection

Ensure Chromosome & FISH analysis Requisition Form (Form 17) is duly filled.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding.

Timeline: 4 Working days

Patient Instructions

1
Before the Test:No special preparation needed, but ensure the requisition form is complete.
2
During the Test:A blood sample will be collected.
3
After the Test:Resume normal activities. Monitor for any discomfort at the puncture site.

About This Test

Who Should Get This Test

To diagnose genetic disorders related to 22q11.2 deletion, such as DiGeorge syndrome and VCFS, enabling timely management and genetic counseling.

How to Prepare

  • No fasting required
  • Fill Form 17
  • Ship at 18-22°C
  • Do not freeze

Doctor's Notes

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

"Early detection of 22q11.2 deletion through FISH testing is vital for managing associated health issues and providing genetic counseling to affected families."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeWhole blood
Sample Volume5 mL (3 mL min.)
ContainerGreen Top (Sodium Heparin) tube
Collection MethodVenipuncture

Sample Stability

Room Temperature: 48 hrs
Refrigerator: Not applicable
Frozen: Not applicable
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume
  • Incorrect tube type

Understanding Your Results

The FISH test result indicates the presence or absence of deletions or duplications in the 22q11.2 region.
📊

Normal

No deletion or duplication detected in 22q11.2 region.

📊

Abnormal

Deletion or duplication detected, indicating possible DiGeorge syndrome or related disorder.

⚠️ When to Consult a Doctor:

If the test result is abnormal, or if symptoms persist, consult a geneticist or pediatrician for further evaluation and management.

Limitations

  • FISH may not detect all types of mutations
  • Cannot detect point mutations

Risks & Considerations

  • Minor bruising at blood draw site
  • Infection (rare)

Interfering Factors

  • Sample contamination
  • Improper sample handling

Frequently Asked Questions

What is the FISH - 22q Deletion Test?
It is a genetic test using Fluorescence In Situ Hybridization to detect deletions or duplications in the 22q11.2 region of chromosome 22, associated with DiGeorge syndrome and VCFS.
Who should take this test?
Individuals with symptoms like heart defects, cleft palate, immune issues, or developmental delays, or those with a family history of related genetic disorders.
How is the sample collected?
A blood sample is drawn from a vein into a Sodium Heparin tube, with no fasting required.
What is the cost of the test?
The cost at DNA Labs India is INR 8000, including free home sample collection across India.
How long does it take to get results?
Results are typically available within 4 working days after sample collection.
What does a positive result mean?
A positive result indicates a deletion or duplication in the 22q11.2 region, which may suggest DiGeorge syndrome or related conditions, requiring further medical evaluation.
Is the test covered by insurance?
Coverage varies by insurance provider; it is not universally covered. Check with your insurer or government schemes like PMJAY or CGHS.
Are there any risks associated with the test?
Risks are minimal, such as minor bruising or infection at the blood draw site, which are rare.
Can this test be done at home?
Yes, free home collection is available for online bookings in many cities across India.
What is DiGeorge syndrome?
DiGeorge syndrome is a genetic disorder caused by a deletion in the 22q11.2 region, leading to symptoms like heart defects, immune problems, and developmental issues.
How accurate is the FISH test?
FISH is a reliable method for detecting deletions and duplications in specific chromosomal regions, but it may not detect all genetic variations.
What should I do if I have symptoms?
Consult a healthcare professional for evaluation; if indicated, they may recommend this test for diagnosis.
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

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.