A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587088



Internal ID6711784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:46097523..46097966hg38UCSC Ensembl
Innerchr11:46119074..46119517hg19UCSC Ensembl
Innerchr11:46075650..46076093hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38444
hg19444
hg18444
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv987535
Supporting Variants
SamplesHuRef
Known GenesPHF21A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587088
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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