A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1175n100



Internal ID20152791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55584048..55641874hg38UCSC Ensembl
chr11:55351524..55409350hg19UCSC Ensembl
chr11:55108100..55165926hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3857827
hg1957827
hg1857827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045853, nsv1041523, nsv1054387, nsv1037894, nsv1043531, nsv1049441
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1175n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer