Structural variant cytogenetic location [Identifier] 81298-2
LOINC Code
| LOINC code | 81298-2 | ||
|---|---|---|---|
| name | Structural variant cytogenetic location [Identifier] | ||
| description | The chromosome region where the structural variant was found, for example, 17p12. This term may be used when more specific information, such as the structural variant reported start-end [LOINC: 81287-5], precision of boundaries [LOINC: 81288-3] and inner and outer start-end [LOINC: 81302-2] and [LOINC: 81301-4], respectively, cannot be or are not reported. | ||
| status | TRIAL | ||
Fully-Specified Name | |||
| component | Structural variant cytogenetic location | ||
| property | ID = Identifier | ||
| 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 cyto loc ID | ||
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. | |||
History/Usage | |||
| first released | |||
| last updated | 2.56 | ||
| last change type | ADD - added | ||
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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