LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Molecular pathology   LP7822-2

Molecular Pathology Panels   LP62072-1

HL7 cytogenetics panels   LP111373-9

Chromosome analysis copy number change panel   LP111372-1

Chromosome analysis copy number change panel | Blood or Tissue | HL7 cytogenetics panels   LP401898-4

Chromosome analysis copy number change panel by Microarray   62343-9

LOINC Code


LOINC code62343-9
nameChromosome analysis copy number change panel by Microarray
descriptionThe microarray chromosome analysis for copy number change
statusACTIVE

Fully-Specified Name

componentChromosome analysis copy number change panel
property-
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.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scale-
methodMicroarray

Additional Names

short nameCMA # change pnl Microarray

Basic Attributes

classPANEL.HL7.CYTOGEN
type1  Laboratory
order vs. observationOrder

Panel Components

62386-8Chromosome analysis summary panel
62374-4Human reference sequence assembly version
62373-6Human reference assembly release, UCSC version [Identifier]
62375-1Microarray platform [Identifier] Narrative
62376-9Microarray platform version number Narrative
62377-7Chromosome copy number change panel
62364-5Test performance information in Specimen Narrative
62365-2Diagnostic impression [Interpretation] in Specimen Narrative
62385-0Recommendation [Interpretation] Document
62366-0Recommended follow-up [Identifier]

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.

Member of these Panels

62389-2Chromosome analysis master panel

History/Usage

test rank9117 of 2000 most commonly performed tests by labs in USA
first released
last updated2.73
last change typeMIN  - change to field other than name
change reasonUpdated Method from "arr.CGH" to "Microarray" based on the ISCN representation of microarray-based methods.

Related Names

arrCGH
Blood
Chrom analy
Chromosom
Chromosomes
CMA # change pnl
Cytogenetics
Exchange
Genetics
Heredity
Heritable
HL7.CYTOGEN
Inherited
Karyotype
 No
Num
Pan
PANEL.HL7.CYTOGEN
Panl
Pnl
Point in time
Random
Replace
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, 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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