A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503407



Internal ID18801688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4560920..4576419hg38UCSC Ensembl
Innerchr11:4582150..4597649hg19UCSC Ensembl
Innerchr11:4538726..4554225hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815500
hg1915500
hg1815500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036169
Supporting Variants
Samples
Known GenesC11orf40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3503407
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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