A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045511



Internal ID19134730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71684611..71816850hg38UCSC Ensembl
Innerchr11:71395657..71527896hg19UCSC Ensembl
Innerchr11:71073305..71205544hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38132240
hg19132240
hg18132240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515293
Samples
Known GenesALG1L9P, FAM86C1, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045511
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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