ADHDgene Database

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Type:

Large-scale studies

Data Summary

Published Variant
- SNP: 1391
- CNV: 398
- Others: 173
Published Gene: 359
Published Region: 128
Pathway by PBA: 8
Study: 361

Detail ...

CNV Report

Basic Info

Name	CNV_Elia[2010]_215
Symbol in Literature	Subject: 130_055_3
Location	chr22:34870070-34916870 (NCBI Build 35 (hg17))
Type	Deletion (hemizygous)
Size	46801 bp
Inheritance	Paternal
Band	22q12.3

CNV related studies (count: 1)

Reference	Author Comments
Elia J, 2010	No excess in the ADHD cohort relative to controls, but matched following criteria: size spanning >=10 consecutive SNPs for deletions and >=20 SNPs for duplications, and present in at least one parent ...... No excess in the ADHD cohort relative to controls, but matched following criteria: size spanning >=10 consecutive SNPs for deletions and >=20 SNPs for duplications, and present in at least one parent along with one or more related probands but not in the healthy control set. More...

Reference

Author Comments

Elia J, 2010

No excess in the ADHD cohort relative to controls, but matched following criteria: size spanning >=10 consecutive SNPs for deletions and >=20 SNPs for duplications, and present in at least one parent ...... No excess in the ADHD cohort relative to controls, but matched following criteria: size spanning >=10 consecutive SNPs for deletions and >=20 SNPs for duplications, and present in at least one parent along with one or more related probands but not in the healthy control set. More...

CNV related genes (count: 2)

Literature-origin genes (count: 0)

Genes from other sources (count: 2)

Approved Symbol	Approved Name	Location	Source
APOL4	apolipoprotein L, 4	22q11.2-q13.2	Mapped by CNV
APOL3	apolipoprotein L, 3	22q13.1	Mapped by CNV

View in gBrowse

Region: chr22:34870070..34916870 (NCBI Build 35 (hg17)) View in gBrowse
(The coordinate of the CNV has been transformed to NCBI Build 37 (hg19) in gBrowse)