PennCNV gene
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| PennCNV | associated_with | CNV | — | 1 |
| PennCNV | targets | CNV | — | 1 |
| PennCNV | targets | copy number variation | — | 1 |
| PennCNV | interacts_with | hidden Markov model | — | 1 |
Mentioned in (6)
Papers in which this entity is mentioned.
- Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays. (2014)
- Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- Expanding the range of ZNF804A variants conferring risk of psychosis. (2011)
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. (2011)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
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 |
|---|---|---|---|
| penncnv | drug | 6 | 22 |
| penncnv | gene | — | — |