A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv211e199



Internal ID20123513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55596916..55697316hg38UCSC Ensembl
chr11:55364392..55464792hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38100401
hg19100401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666582, esv2676819, esv2669097
SamplesNA11881, NA12827, HG00359, NA12043, NA07347, NA12750, NA12748, NA11930, NA20522, NA20527, NA20503, NA12342, NA11920, NA12347, NA20544, NA20796, NA20535, NA20508, NA11918, NA06989, NA10847, NA12340, NA20816, NA12828, NA20778, NA20786, NA12058, NA20539, NA20805, NA12776, NA20798, NA12341, NA20521, NA12414, NA20532, NA20761, NA20505, NA12763, NA12843, NA20533, NA20819, NA12282, NA20515, NA12383, NA20811, NA07357, NA20504, NA20530, NA20783, NA20801, NA20754, NA07048, NA12761, NA11831, NA11894, NA20520, NA20589, NA12006, NA20769, NA07346, NA12046, NA20760, NA20512, NA12348, NA20795, NA12275, NA20540, NA20814, NA20774, NA20815, NA20797, NA20582, NA20766, NA11832, NA20525, NA20581, NA20537, NA06984, NA20518, NA20509, NA20507, NA11992, NA12003, NA20810, NA12399, NA20812, NA20758, NA11829, NA20768, NA20524, NA20804, NA06994, NA20502, NA20538, NA12775
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv211e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss95
Observed Complex0
Frequencyn/a


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