| CLASS | HL7.CYTOGEN | LP111381-2 |
| COMPONENT | Chromosome copy number change | LP111402-6 |
| PROPERTY | Type | LP6886-8 |
| TIME_ASPCT | Pt | LP6960-1 |
| SYSTEM | Bld/Tiss | LP7061-7 |
| SCALE_TYP | Nom | LP7750-5 |
| METHOD_TYP | Molgen | LP6404-0 |
| AnswerList | CopyNumberChangeType | LL1041-4 |
| parent | Chromosome copy number change | Blood or Tissue | HL7 cytogenetics | LP410578-1 |
| CLASSTYPE | Laboratory class | |
| ORDER_OBS | Observation | |
| UNITSREQUIRED | N |
| LONG_COMMON_NAME | en-US | Chromosome copy number change [Type] |
| LONG_COMMON_NAME | en-US | Chromosome copy number change [Type] |
| SHORTNAME | en-US | Chrom copy # change |
| ConsumerName | en-US | Chromosome copy number change, Blood or tissue specimen |
| LONG_COMMON_NAME | fr-FR | Variabilité nombre de copies chromosomiques [Type] Sang/Tissu ; Résultat nominal ; Biologie moléculaire |
| LONG_COMMON_NAME | nl-NL | Wijziging in aantal kopieën van chromosoom [type] in bloed of weefsel d.m.v. moleculair genetisch onderzoek |
| LONG_COMMON_NAME | es-MX | Cambio del número de copias de cromosomas: Sangre o tejido : Punto temporal: Tipo: Nominal: Genética molecular |
LOINC Version: 2.77
FHIR