A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv1154761

Internal ID

22085266

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:93964890..93968426	hg38	UCSC Ensembl
Outer	chr11:93964792..93971294	hg38	UCSC Ensembl
Inner	chr11:93698056..93701592	hg19	UCSC Ensembl
Outer	chr11:93697958..93704460	hg19	UCSC Ensembl

Cytoband

11q21

Allele length

Assembly	Allele length
hg38	6503
hg19	6503

Variant Type

OTHER complex

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

nssv4007245, nssv4007244, nssv4007243, nssv4007249, nssv4007251, nssv4007246, nssv4007252, nssv4007247, nssv4007248, nssv4007250

Samples

Known Genes

Method

SNP array

Analysis

Default settings

Platform

Comments

Reference

Lou_et_al_2014

Pubmed ID

Accession Number(s)

Frequency

Sample Size	131
Observed Gain	1
Observed Loss	9
Observed Complex	0
Frequency	n/a