A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1241n100



Internal ID22787328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81271207..81307644hg38UCSC Ensembl
chr11:80982250..81018687hg19UCSC Ensembl
chr11:80659898..80696335hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3836438
hg1936438
hg1836438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048313, nsv1035986, nsv1053989, nsv1053742, nsv1047389, nsv1043852, nsv1038253, nsv1040869, nsv1053083
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)dgv1241n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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