copy number variations variant
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| copy number variations | risk_factor_for | OCD | — | 1 |
Mentioned in (11)
Papers in which this entity is mentioned.
- Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
- Application of third-generation sequencing in cancer research. (2021)
- Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
- Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes. (2020)
- Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
- Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
- Integrated analysis of gene expression and copy number identified potential cancer driver genes with amplification-dependent overexpression in 1,454 solid tumors. (2017)
- The PsychENCODE project. (2015)
- Integrative clinical genomics of advanced prostate cancer. (2015)
- Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
- DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing. (2010)
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 variations | variant | 19 | 21 |
| rare potentially damaging copy number variations | variant | — | — |