A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665710



Internal ID9931815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119243299..119245574hg38UCSC Ensembl
Outerchr11:119243113..119245775hg38UCSC Ensembl
Innerchr11:119114009..119116284hg19UCSC Ensembl
Outerchr11:119113823..119116485hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6311309
SamplesHG00232
Known GenesCBL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665710
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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