A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1104n100



Internal ID22787191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39341045..39386915hg38UCSC Ensembl
chr11:39362595..39408465hg19UCSC Ensembl
chr11:39319171..39365041hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3845871
hg1945871
hg1845871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040161, nsv1052455, nsv1048480
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)dgv1104n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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