A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035877



Internal ID19125096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41796604..41816640hg38UCSC Ensembl
Innerchr11:41818154..41838190hg19UCSC Ensembl
Innerchr11:41774730..41794766hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3820037
hg1920037
hg1820037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503123
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035877
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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