Chromosome analysis in Blood by Microarray 107159-6
LOINC Code
LOINC code | 107159-6 | ||
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name | Chromosome analysis in Blood by Microarray | ||
description | This term represents chromosomal analysis by microarray is a high-resolution method for detecting genomic copy number changes and structural variations in blood samples. This technique can identify aneuploidies, deletions, duplications, and other chromosomal abnormalities across the entire genome. Microarray analysis provides detailed information on copy number variations and can detect submicroscopic aberrations that may not be visible through conventional karyotyping. [PMID: 24053112] | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Chromosome analysis | ||
property | Find = Finding | ||
time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
system | Bld = Whole blood | ||
scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
method | Microarray | ||
Additional Names | |||
short name | Chrom analy Bld Microarray | ||
Basic Attributes | |||
class | MOLPATH | ||
type | 1 Laboratory | ||
order vs. observation | Both | ||
Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
first released | |||
last updated | 2.79 | ||
last change type | ADD - added | ||
Related Names | |||
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