86611-1

LOINC Code


LOINC code86611-1
name
descriptionChromosome analysis results by microarray can detect aneuploidy, other structural variations, microdeletions and microduplications. This term was created for, but not limited in use to CytoScan HD Array by ThermoFisher Scientific. The test detects high resolution copy numbers across the genome that provide allelic imbalance information from single nucleotide polymorphisms.
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.
systemAmnio fld/CVS
    Amnio fld  =  Amniotic fluid
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodMicroarray

Additional Names

short nameAF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; arrCGH; Chorionic villi; Chorionic villus sample; Chrom analy; Chromosom; Chromosomes; Cytogenetics; Document; Finding; Findings; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Kar

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationChrom analy Amn

History/Usage

first released
last updated2.65
last change typeMIN  - change to field other than name

Related Names



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.

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