FISH for 17P (TP53) Abnormalities
Overview of FISH for 17P (TP53) Abnormalities in Kollam
What is the FISH for 17p (TP53 Abnormalities) test?
This test uses fluorescence in situ hybridization (FISH) to detect deletions or abnormalities in the TP53 gene on chromosome 17p.
Why is the test performed?
To evaluate prognosis and therapeutic options in cancers like chronic lymphocytic leukemia (CLL).
What sample is needed, and how is it collected?
Blood or bone marrow aspirates are used for FISH analysis.
How are the results interpreted?
Presence of TP53 deletion indicates poor prognosis and potential resistance to standard therapies.
Is any special preparation needed before the test?
No preparation is needed.
Test included
- Specimen
- Clinical Indications
- Total Number Of Cells
- Tp53 Deletion
- Normal
- Interpretation
Doctor information
Test code
7644
CPT and Loinc codes
Department
- Cytogenetics
Turn around time
7 Working Days
Test run frequency
Every Day TIME - 07:00
Performing locations
3 labs across India
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Bone Marrow Heparin | Green Vacutainer | 2 ML |
| Heparin Whole Blood | Green Vacutainer | 2 ML |
Specimen stability information
Bone Marrow Heparin, Heparin Whole Blood
Collection instructions
Specimen To Reach Us Within 24-48 Hrs After Collection. [Please Mention The Clinical History, Blood Picture (Cbc Report) And Medication Of The Patient On The Trf]
Test price
₹6000
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₹6000