Detail Information of AutCNV0000723

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	-	-	-	-	223	-	223	Bremer, 2011
Population:	-
Platform:	Agilent 244K oligonucleotide CGH microarray, 33K and 38K BAC arrays
Method:	aCGH
Marker:	-
Band:	22q11.21-q11.22
Evidences:	Overlapping/Recurrent CNVs; Denovo CNVs;
Region:	Chr22: 21470000-23070000 (hg18: Chr22: 19800000-21400000)
Gain/Loss:	loss

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
AutG5594	MAPK1	0	0	1	0	1	1	14
AutG7332	UBE2L3	0	0	0	1	1	1	5
AutG23753	SDF2L1	0	0	0	1	1	1	5
AutG9647	PPM1F	0	0	0	1	1	0	3

Simple Query:

Paper Collected: 6/30/2018

Last Update: 8/26/2018