ADHDgene Database
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Type:
  • Large-scale studies
  • Data Summary
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

CNV Report

Basic Info
Name CNV_Lionel[2011]_19
Symbol in Literature Sample:87600.3_97kb
Location chr4:0-0 (NCBI36 / hg18)
Type Loss
Size 97 bp
Inheritance M
Band 4p16

CNV related studies (count: 1)
Reference Author Comments
Lionel, A. C., 2011 Rare CNVs at loci implicated in other neurodevelopmental disorders. Precious reported for Mild intellectual disability. Rare CNVs at loci implicated in other neurodevelopmental disorders. Precious reported for Mild intellectual disability.

CNV related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 1)


View in gBrowse

Region: chr4:0..0 (NCBI36 / hg18) View in gBrowse
(The coordinate of the CNV has been transformed to NCBI Build 37 (hg19) in gBrowse)
View in gBrowse

Copyright: Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences Feedback
Last update: Feb 26, 2014