A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552861



Internal ID15993584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:589246..662407hg38UCSC Ensembl
Innerchr11:589246..662407hg19UCSC Ensembl
Innerchr11:579246..652407hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3873162
hg1973162
hg1873162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763556
Samples
Known GenesCDHR5, DEAF1, DRD4, IRF7, PHRF1, SCT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552861
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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