LOINC Code 95069-1: Chr 1q and 9 and 11 and 15 aneuploidy and 13q del FISH Doc (BM)
95069-1 is a LOINC code used to identify Chr 1q and 9 and 11 and 15 aneuploidy and 13q del FISH Doc (BM) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Chromosome 1q & 9 & 11 & 15 aneuploidy & chromosome region 13q deletion. It is commonly used with the system or sample type Bone mar.
What is this code?
LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Chromosome 1q & 9 & 11 & 15 aneuploidy & chromosome region 13q deletion. It is commonly used with the system or sample type Bone mar.
When is it used?
- Used in lab systems, EHRs, and clinical data exchange.
- May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
- Status: ACTIVE
- Order vs observation: Both
- Method: FISH
What it does not mean
- The code identifies the observation or test, not the actual result.
Key facts
- Chromosome 1q and 9 and 11 and 15 aneuploidy and 13q deletion in Bone marrow by FISH
- Chromosome 1q & 9 & 11 & 15 aneuploidy & chromosome region 13q deletion
- The detection by FISH analysis of gains (duplications, aneuploidy) and losses (deletion or monosomy) of chromosome regions (e.g. 1q, 13q, 9, 11 and 15) associated with multiple myeloma. This study is performed to determine the prognostic risk for disease outcome. For example, gains of chromosome 1q and monosomy or deletions of 13q are associated with less favorable outcomes whereas gains of chromosome 9, 11, and 15 are associated with more favorable outcomes.
- BM; BON; Bone marrow; Chr 1q+9+11+15 aneu 13q; Chr 1q+9+11+15 aneu 13q Del; Chromosom; Chromosomes; Cyto loc; Del; Deletions; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; MAR; Marrow (bone); minimal angle of resolution; Minimum angle of resolution; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random
Where you may see this code
You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.
Common synonyms
Frequently asked questions
About this content
This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.