A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054705



Internal ID18797236
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 StatusM
Merged Variants
Supporting Variantsnssv3706407, nssv3510786, nssv3502949
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)nsv1054705
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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