A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659739



Internal ID9925844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59853923..59854447hg38UCSC Ensembl
chr11:59621396..59621920hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6410177, essv6488915, essv6032769, essv6316375, essv6245625, essv6223839, essv5836550, essv5683707, essv6370780, essv5633584, essv6126296, essv5514500, essv6575228, essv5734870, essv6366287, essv6409942, essv5838026, essv5717309, essv5808975, essv5649673, essv6425628
SamplesNA18508, NA18526, NA19379, HG01366, NA18489, NA19130, NA19172, NA19200, NA19347, NA18981, NA18523, NA18858, NA19436, NA18517, NA19311, NA19376, NA19438, NA19093, NA18511, NA18522, HG01061
Known GenesTCN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659739
Frequency
Sample Size1151
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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