Detail Information of AutCNV0000204


Users can click the chromosome coordinates of "Region" label to view information in UCSC Genome Browser.
Ancestry | ADI-R | ADOS | Diagnosis | Family | Individual | Reference | |||||
---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | |||||
Mixed | ![]() | ![]() | ASD | 397 | 35 | 362 | - | 397 | 372 | 769 | Christian, 2008 |
Population: | USA | ||||||||||
Platform: | RPCI 19K BAC array | ||||||||||
Method: | aCGH | ||||||||||
Marker: | - | ||||||||||
Band: | 2p15 | ||||||||||
Evidences: | CNVs Only Present In Patients; | ||||||||||
Region: | Chr2: 62258229-63028719 (hg18: Chr2: 62111733-62882223) | ||||||||||
Gain/Loss: | gain |


Abbreviations: AD, autosomal dominant; AR, autosomal recessive; ASD, autism spectrum disorder; ID, intellectual disability; XL, X linked.
Gene ID | Gene Symbol | Inheritance | Evidence Level |
---|---|---|---|
No data! |


Gene ID | Gene Symbol | Evidence Score | Total Score | |||||
---|---|---|---|---|---|---|---|---|
Low-Scale Association | GWAS | Low-Scale Single Gene | Expression | CNV | Linkage | |||
AutG10678 | B3GNT2 | 0 | 0 | 0 | 1 | 0 | 0 | 1 |