A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706407



Internal ID19004688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4560920..4666008hg38UCSC Ensembl
Innerchr11:4582150..4687238hg19UCSC Ensembl
Innerchr11:4538726..4643814hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38105089
hg19105089
hg18105089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054705
Supporting Variants
Samples
Known GenesC11orf40, OR51D1, OR51E1, OR52I1, OR52I2, TRIM68
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706407
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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