A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989051



Internal ID12979283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81777987..82049063hg38UCSC Ensembl
Innerchr11:81489029..81760105hg19UCSC Ensembl
Innerchr11:81166677..81437753hg18UCSC Ensembl
Innerchr11:81166677..81437753hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38271077
hg19271077
hg18271077
hg17271077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34646
Supporting Variants
SamplesNA12753
Known GenesMIR4300
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989051
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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