ADHDgene Database

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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_Lesch[2011]_1
Symbol in Literature	Patient: 991 (male)
Location	chr3:166944967-168896272 (NCBI Build 35 (hg17))
Type	Deletion
Size	1951305 bp
Inheritance	De novo
Band	3q26.1

CNV related studies (count: 1)

Reference	Author Comments
Lesch KP, 2011	The aberrations are likely ADHD-associated, based on the fact that they are not documented in the reference data sets. The aberrations are likely ADHD-associated, based on the fact that they are not documented in the reference data sets.

CNV related genes (count: 5)

Literature-origin genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
ZBBX	zinc finger, B-box domain containing	3q26.1	1(0/0/1)

Genes from other sources (count: 4)

Approved Symbol	Approved Name	Location	Source
PDCD10	programmed cell death 10	3q26.1	Mapped by CNV
WDR49	WD repeat domain 49	3q26.1	Mapped by CNV
BCHE	butyrylcholinesterase	3q26.1-q26.2	Mapped by CNV
SERPINI2	serpin peptidase inhibitor, clade I (pancpin), member 2	3q26	Mapped by CNV

View in gBrowse

Region: chr3:166944967..168896272 (NCBI Build 35 (hg17)) View in gBrowse
(The coordinate of the CNV has been transformed to NCBI Build 37 (hg19) in gBrowse)