A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422214



Internal ID7906311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64545019..64715946hg38UCSC Ensembl
Innerchr11:64312491..64483418hg19UCSC Ensembl
Innerchr11:64069067..64239994hg18UCSC Ensembl
Innerchr11:64069067..64239994hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38170928
hg19170928
hg18170928
hg17170928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161405
SamplesND04575
Known GenesNRXN2, SLC22A11, SLC22A12
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422214
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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