96984-0

LOINC Code


LOINC code96984-0
name
descriptionChromosome analysis by microarray can detect aneuploidy, triploidy, deletions/duplication, uniparental disomy (UPD), and other structural variations. Single nucleotide polymorphisms (SNP)-based analysis is used to detect high resolution copy numbers across the genome to detect allelic imbalance information.
statusACTIVE

Fully-Specified Name

componentChromosome analysis
propertyFind  =  Finding
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemPOC
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodMicroarray

Additional Names

short namearrCGH; Chrom analy; Chromosom; Chromosomes; Cytogenetics; Document; Finding; Findings; Gyn; Gynecology; Karyotype; Molecular pathology; MOLPATH; OB; ObGyn; Obstetrics; Point in time; Products of Conception; Random

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationChrom analy POC

History/Usage

first released
last updated2.7
last change typeADD  - added

Related Names

N

Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.

Aimee - AI-powered coding assistant Would you like Aimee - AI
to help you with this?