A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661166



Internal ID9927271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66116676..66117107hg38UCSC Ensembl
Outerchr11:66116519..66117260hg38UCSC Ensembl
Innerchr11:65884147..65884578hg19UCSC Ensembl
Outerchr11:65883990..65884731hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6271802, essv6455529, essv5565850, essv6089266, essv6474657, essv5538699, essv6240438, essv6089444, essv5445298, essv5798851, essv6579302, essv5730358, essv5832684, essv5624243, essv5570645
SamplesNA19359, HG01051, NA19448, NA19457, NA19471, NA19437, NA19707, NA18516, NA19114, NA19440, NA19390, NA19380, NA18522, NA19429, NA18487
Known GenesPACS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661166
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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