Chromosome copy number change panel 62377-7
LOINC Code
LOINC code | 62377-7 | ||
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name | Chromosome copy number change panel | ||
description | The panel code that is used to contain the details about the copy number pain, such as the base pair start and end coordinates of where the change occurred. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Chromosome copy number change panel | ||
property | - | ||
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/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
scale | - | ||
method | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
short name | Chrom copy # change pnl | ||
Basic Attributes | |||
class | PANEL.HL7.CYTOGEN | ||
type | 1 Laboratory | ||
order vs. observation | Order | ||
Panel Components | |||
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 | |||
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History/Usage | |||
first released | |||
last updated | 2.61 | ||
last change type | MIN - change to field other than name | ||
Related Names | |||
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