A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796250



Internal ID18835361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602849..55624962hg38UCSC Ensembl
Innerchr11:55370325..55392438hg19UCSC Ensembl
Innerchr11:55126901..55149014hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3822114
hg1922114
hg1822114
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892008
Supporting Variants
Samples
Known GenesOR4C11
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796250
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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