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FISH, p53, Deletion 17p13.1

Order Code: P53FSH

Test Summary

Loss of the p53 gene, located in chromosome 17p13.1, is a common occurrence in neoplastic disorders, including hematologic disorders. FISH studies for deletion p53 are performed in addition to G-banding analysis of bone marrow, hematologic blood, lymph nodes, and solid tumors. This probe may be useful in detecting loss of p53 in complex karyotypes. Deletion of p53 is an adverse prognostic marker in CLL and follicular lymphoma.

Aliases

  • N/A

Specimen Collection

Order Code

P53FSH

EPIC (Premier) Code

LAB6340

Includes

N/A

CPT Code

  • 88271 (x2)
  • 88275

Billing Code

  • 670944
  • 670945

CPT Statement

Methodology

Fluorescence In Situ Hybridization (FISH)

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly VA, 20153

Department

Reference Testing

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Monday - Sunday morning; Report available: 5 days

Specimen Collection

Billing

CPT Code

  • 88271 (x2)
  • 88275

Billing Code

  • 670944
  • 670945

CPT Statement

Result Information

Methodology

Fluorescence In Situ Hybridization (FISH)

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Monday - Sunday morning; Report available: 5 days