Test ID: FP73
1p36.3 Microdeletion Syndrome, FISH
Secondary ID 
A test code used for billing and in test definitions created prior to November 2011
88541
Useful For Suggests clinical disorders or settings where the test may be helpful
As an aid in the diagnosis of 1p microdeletion syndrome, in conjunction with #8696 Chromosome Analysis, for Congenital Disorders, Blood
Detecting cryptic translocation involving 1p36.3 that are not demonstrated by conventional chromosome studies
Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test
Method Name A short description of the method used to perform the test
Fluorescence In Situ Hybridization (FISH)
Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name
1p36.3 Del, FISH
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