FISH FOR 17P (TP53) ABNORMALITIES

This test detects abnormalities in chromosome 17p, specifically the TP53 gene, which is involved in tumor suppression. TP53 mutations are associated with various cancers, including breast, lung, and colorectal cancer. This test aids in cancer diagnosis and prognosis.

Also known asChromosome 17p (tp53) Abnormalities Chromosome 17p (tp53) Abnormalities

Available via

Home Collection, Lab Visit

Contains

6 parameters

Earliest reports in

7 Working Days

Test details

FISH FOR 17P (TP53) ABNORMALITIES Test in Bengaluru Overview

Preparations

No special preparations needed

Test included
FISH FOR 17P (TP53) ABNORMALITIES includes 6 parameters

  • Specimen
  • Clinical Indications
  • Total Number Of Cells
  • Tp53 Deletion
  • Normal
  • Interpretation
Frequently Asked Questions

This test uses fluorescence in situ hybridization (FISH) to detect deletions or abnormalities in the TP53 gene on chromosome 17p.

To evaluate prognosis and therapeutic options in cancers like chronic lymphocytic leukemia (CLL).

Blood or bone marrow aspirates are used for FISH analysis.

Presence of TP53 deletion indicates poor prognosis and potential resistance to standard therapies.

No preparation is needed.

Test code

7644

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Bone Marrow HeparinGreen Vacutainer2 ML
Heparin Whole BloodGreen Vacutainer2 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]

Specimen rejection criteria

Test run frequency

Every Day TIME - 07:00

Turn around time

7 Working Days

Performing locations

Department

  • Cytogenetics

CPT and Loinc codes

FISH FOR 17P (TP53) ABNORMALITIES

3000