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]_4
Symbol in Literature	Patient: 241 (male)
Location	chr5:60069539-60353244 (NCBI Build 35 (hg17))
Type	Deletion
Size	283705 bp
Inheritance	Maternal (affected)
Band	5q12.1

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: 3)

Literature-origin genes (count: 0)

Genes from other sources (count: 3)

Approved Symbol	Approved Name	Location	Source
NDUFAF2	NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 2	5q12.1	Mapped by CNV
ERCC8	excision repair cross-complementing rodent repair deficiency, complementation group 8	5q12.1	Mapped by CNV
ELOVL7	ELOVL fatty acid elongase 7	5q12	Mapped by CNV

View in gBrowse

Region: chr5:60069539..60353244 (NCBI Build 35 (hg17)) View in gBrowse
(The coordinate of the CNV has been transformed to NCBI Build 37 (hg19) in gBrowse)