16p11.2 duplication variant
Evidence from:
primary |
all sources
Related entities (15)
Mentioned in (8)
Papers in which this entity is mentioned.
- Opposite effects on facial morphology due to gene dosage sensitivity. (2014)
- Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
- Distribution of disease-associated copy number variants across distinct disorders of cognitive development. (2013)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. (2011)
- Large copy-number variations are enriched in cases with moderate to extreme obesity. (2010)
- Growth of white matter in the adolescent brain: role of testosterone and androgen receptor. (2008)
Merged raw entities (7)
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 |
|---|---|---|---|
| 16p11.2 duplication | variant | 8 | 25 |
| 16p11.2 cnv duplication | variant | — | — |
| 16p11.2 dup | variant | — | — |
| 16p11.2 duplications | variant | — | — |
| chromosome 16p11.2 duplication | variant | — | — |
| duplications of chr16p11.2 | variant | — | — |
| reciprocal duplication of 16p11.2 | variant | — | — |