A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1206n100



Internal ID22787293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55916509..56061980hg38UCSC Ensembl
chr11:55683985..55829456hg19UCSC Ensembl
chr11:55440561..55586032hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38145472
hg19145472
hg18145472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053326, nsv1043632, nsv1053027, nsv1053592, nsv1050801, nsv1048070, nsv1042542, nsv1047031, nsv1053583, nsv1048664, nsv1036558
Samples
Known GenesOR10AG1, OR5AS1, OR5F1, OR5I1, OR7E5P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1206n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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