Detail Information of AutCNV0004263

1. Sample AND Method Top

Users can click the chromosome coordinates of "Region" label to view information in UCSC Genome Browser.

Ancestry	ADI-R	ADOS	Diagnosis	Family				Individual			Reference
Ancestry	ADI-R	ADOS	Diagnosis	Total	Simplex	Multiplex	Control	Affected	Control	Total	Reference
Caucasion	-	-	ASD	1127	1127	-	-	-	-	-	Sanders, 2011
Population:	Simons Simplex Collection
Platform:	Illumina Infinium 1M SNP array
Method:	SNP microarray
Marker:	-
Band:	7q11.23
Evidences:	Overlapping/Recurrent CNVs;
Region:	Chr7: 72717647-74144177 (hg18: Chr7: 72355583-73782113)
Gain/Loss:	gain

2. Related Syndromic Genes Top

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!

3. Related Non-syndromic Genes Top

Gene ID	Gene Symbol	Evidence Score						Total Score
Gene ID	Gene Symbol	Low-Scale Association	GWAS	Low-Scale Single Gene	Expression	CNV	Linkage	Total Score
AutG6804	STX1A	2	0	1	1	0	0	15
AutG2969	GTF2I	1	0	1	0	1	0	14
AutG3984	LIMK1	0	0	0	1	0	0	11
AutG2006	ELN	0	1	0	0	0	0	4

Simple Query:

Paper Collected: 6/30/2018

Last Update: 8/26/2018