Test Overview
Test Methodology

Fluorescence In Situ Hybridization (FISH)

Test Usage

FISH testing is intended to determine inheritance of an abnormal Chromosomal Microarray Analysis result on a child/proband (CMA testing available from the MMGL Molecular Genetics Laboratory). FISH analyses of peripheral blood samples from both parents of a patient with a CMA aberration are recommended to determine whether the abnormality occurred de novo or was inherited from a carrier parent. Identifying the origin of the aberration (de novo or parental) allows a better assessment of the probability that the aberration is pathogenic, promotes improved diagnosis of disease (or risk of disease), allows a more precise calculation of recurrence risk, and facilitates more accurate and appropriate counseling.

Reference Range *

Interpretive report provided.

* Reference ranges may change over time. Please refer to the original patient report when evaluating results.

Test Details
Days Set Up
Monday - Friday, 8:00am - 4:00pm
Soft Order Code
CGNFC
MiChart Code
Cytogenetics, FISH for CMA-detected Abnormality, Peripheral Blood
Synonyms
  • CGNFC
  • Chromosomal Microarray Confirmation
  • FISH Confirmation, Parental Sample
  • CMA Confirmation
  • Parental Analysis of Chromosomal Microarray Result
  • Array Analysis, Parental Sampl
  • CMCAP
  • Parent Analysis of CMA Result
  • FISH ANALYSIS, PRNTL SAMPLE
  • CMFAP
  • CMAPAS
  • Parental FISH
  • CMFAPS
  • FISH Analysis, Prntl Shadow
  • CGNFC
  • Cytogenetics, FISH for CMA Abn
  • Aberrant CMA confirmation by FISH
  • Aberrant Chromosomal Microarray (CMA) Confirmation by FISH
Laboratory
Cytogenetics
Section
Cytogenetics
Specimen Requirements
Collection Instructions

Please notify MLabs Client Services Center prior to sending specimen. Requests for this test will be accepted if the CMA test was performed for the child/proband at the University of Michigan MMGL Molecular Genetics Laboratory. Collect specimen in a green top (sodium heparin) tube. Invert the tube several times to prevent clotting. Send the specimen intact at room temperature within 24 hours of collection. DO NOT CENTRIFUGE. Clotted or hemolyzed specimens are unacceptable. Include the proband's CMA information specified, as follows: Proband name, U of M registration number, chromosome abnormality (deletion or duplication), size, band, beginning and ending nucleotide numbers.

Rejection Criteria
Clotted or hemolyzed specimen, or specimen over 48 hours old.
Normal Volume
5 mL whole blood
Minimum Volume
2 mL whole blood
Additional Information

For additional information on FISH for CMA-detected Abnormality, contact the UMHS/MLabs Cytogenetics Laboratory. Chromosome Analysis (cpt codes 88230 and 88262) will be performed if indicated. By ordering this test the clinician acknowledges that additional reflex testing will be performed and billed at a separate additional charge if indicated.

Billing
CPT Code
88230, 88271, 88273 (deletion) or 88275 (duplication)
Fee Code
21571, 36538, 21572 (deletion) or 21573 (duplication)
Resources