copy-number variants variant
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (2)
Papers in which this entity is mentioned.
- ACMG clinical laboratory standards for next-generation sequencing. (2013)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
Merged raw entities (1)
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 variants | variant | 6 | 6 |