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_Lesch[2011]_17
Symbol in Literature	Patient: 211 (male)
Location	chr12:7894681-8009303 (NCBI Build 35 (hg17))
Type	Duplication
Size	114622 bp
Inheritance	Maternal (affected)
Band	12p13.31

CNV related studies (count: 1)

Reference	Author Comments
Lesch KP, 2011	One of the additional four CNVs detected that the authors considered potentially syndrome-associated despite the fact that they did not reach the high-stringency threshold scores because they were als...... One of the additional four CNVs detected that the authors considered potentially syndrome-associated despite the fact that they did not reach the high-stringency threshold scores because they were also observed at low frequency in one or both of the reference data sets. More...

Reference

Author Comments

Lesch KP, 2011

One of the additional four CNVs detected that the authors considered potentially syndrome-associated despite the fact that they did not reach the high-stringency threshold scores because they were als...... One of the additional four CNVs detected that the authors considered potentially syndrome-associated despite the fact that they did not reach the high-stringency threshold scores because they were also observed at low frequency in one or both of the reference data sets. More...

CNV related genes (count: 2)

Literature-origin genes (count: 0)

Genes from other sources (count: 2)

Approved Symbol	Approved Name	Location	Source
SLC2A14	solute carrier family 2 (facilitated glucose transporter), member 14	12p13.31	Mapped by CNV
SLC2A3	solute carrier family 2 (facilitated glucose transporter), member 3	12p13.3	Mapped by CNV

View in gBrowse

Region: chr12:7894681..8009303 (NCBI Build 35 (hg17)) View in gBrowse
(The coordinate of the CNV has been transformed to NCBI Build 37 (hg19) in gBrowse)