Variant Details

Variant: esv2386638

Internal ID

8057749

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:10271200..10272298	hg38	UCSC Ensembl
Outer	chr11:10271021..10272493	hg38	UCSC Ensembl
Inner	chr11:10292747..10293845	hg19	UCSC Ensembl
Outer	chr11:10292568..10294040	hg19	UCSC Ensembl
Inner	chr11:10249323..10250421	hg18	UCSC Ensembl
Outer	chr11:10249144..10250616	hg18	UCSC Ensembl

Cytoband

11p15.4

Allele length

Assembly	Allele length
hg38	1473
hg19	1473
hg18	1473

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4580592

Samples

NA18507

Known Genes

SBF2

Method

Sequencing

Analysis

Hierarchical clustering of anomalous readpairs was used to identify groupings of five or more readpairs that had a similar size and position. Read pairs were defined as anomalous if they had high-confidence alignments of each individual read that nevertheless were either incorrectly oriented or implied an insert size of at least 3 standard deviations outside the sample median.

Platform

Not specified

Comments

Reference

Bentley_et_al_2008

Pubmed ID

18987734

Accession Number(s)

esv2386638

Frequency

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