Variant analysis method [Type] 81304-8
LOINC Code
| LOINC code | 81304-8 | ||||||
|---|---|---|---|---|---|---|---|
| name | Variant analysis method [Type] | ||||||
| description | The method used for analyzing chromosome structural variation, such as FISH, arrCGH, sequencing, and MLPA. | ||||||
| status | TRIAL | ||||||
Fully-Specified Name | |||||||
| component | Structural variant analysis method | ||||||
| property | Type = Type: The Property Type is used for assays that identify the specific analyte in cases when the baseline presence of the analyte is known. | ||||||
| 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 | ^Patient | ||||||
| scale | Nom = Nominal: Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody. | ||||||
| method | * | ||||||
Additional Names | |||||||
| short name | Struct var analysis method | ||||||
Basic Attributes | |||||||
| class | MOLPATH | ||||||
| type | 1 Laboratory | ||||||
| order vs. observation | Observation | ||||||
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 | 2.58 | ||||||
| last change type | MIN - change to field other than name | ||||||
Related Names | |||||||
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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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