A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051057



Internal ID18793588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60694023..60731810hg38UCSC Ensembl
Innerchr11:60461496..60499283hg19UCSC Ensembl
Innerchr11:60218072..60255859hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3837788
hg1937788
hg1837788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513440, nssv3518767, nssv3503869
Samples
Known GenesMS4A8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051057
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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