Copy number variation (CNV) variant
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (2)
Papers in which this entity is mentioned.
- Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
- The impact of structural variation on human gene expression. (2017)
Merged raw entities (2)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| copy number variation (cnv) | variant | 4 | 4 |
| rare cnv alleles | variant | — | — |