A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040084



Internal ID18782615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122887702..122911090hg38UCSC Ensembl
Innerchr11:122758410..122781798hg19UCSC Ensembl
Innerchr11:122263620..122287008hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3823389
hg1923389
hg1823389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511739
Samples
Known GenesC11orf63
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040084
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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