A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666484



Internal ID9932589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26300925..26301168hg38UCSC Ensembl
chr11:26322472..26322715hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5874008, essv6050991, essv5692019, essv5595191, essv5965164, essv5641924, essv6541376, essv5898985, essv5454566, essv5571040, essv5915525, essv5813028, essv5642592, essv6460767, essv5562582, essv6160079, essv6438881, essv5689509, essv5810687, essv5562350, essv5731563, essv6067272, essv5763277, essv6359285, essv5771552, essv5401134, essv5399965, essv6155925, essv5534483, essv6234790, essv6071710, essv6518669, essv5752668, essv6258200, essv6589376, essv6052393, essv5583908, essv6141136, essv6226383, essv6073660, essv5888948, essv6291843, essv5723525, essv6242270, essv5850752, essv5649744, essv6281455, essv6541052, essv6257786, essv5541119, essv5617219, essv6204529, essv5946769, essv5621577, essv5799175, essv5675039, essv5566490, essv5961692, essv6381034, essv5598797, essv6323904, essv6451755, essv5763476, essv5444813, essv6135011, essv5589072, essv5582230, essv6535148, essv5569191, essv6453851, essv5884596, essv5465195, essv6495231, essv6435023, essv6352921, essv6010829, essv5419461, essv5855011, essv6330383, essv5576268, essv6342076, essv6274345, essv5891342, essv5414150, essv5638904, essv5614869, essv5713012, essv5582168, essv5506353, essv5784120, essv6221996, essv5784836, essv5700837, essv5737182, essv5427236, essv5399082, essv6287471, essv6324332, essv6064919
SamplesNA19700, NA19703, HG00249, NA18508, NA19399, NA18507, NA18999, NA18917, NA18603, NA20294, NA19355, NA19377, HG00115, HG00654, NA19920, NA18627, NA19374, HG00689, HG00448, NA18567, HG00330, NA18571, NA19054, HG00185, NA18964, NA20291, NA19130, NA20278, NA19917, HG00232, NA19371, NA19238, NA18560, NA19235, NA18617, NA19172, NA18986, NA19189, NA18557, NA19456, NA19445, HG00326, HG00530, NA18544, NA19908, NA19247, NA19437, HG00428, NA19462, NA19347, NA18933, HG00653, NA18956, NA19391, NA19327, NA19236, NA20126, NA18910, NA18548, NA19461, HG00373, HG00463, NA19395, NA18541, NA18608, HG00476, NA19390, NA18543, HG00625, NA20276, HG00580, HG00734, HG00136, NA19240, NA19380, NA19010, NA19428, NA19311, NA19467, NA20803, HG00418, HG00620, NA19376, NA19398, HG00672, NA19248, NA19438, NA18987, HG00342, NA19716, HG00267, NA18983, HG01377, NA19755, NA18488, NA19312, HG01125, NA19065, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666484
Frequency
Sample Size1151
Observed Gain0
Observed Loss99
Observed Complex0
Frequencyn/a


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