Variant Details

Variant: essv4691769

Internal ID

7277401

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:64371936..64372028	hg38	UCSC Ensembl
Outer	chr15:64371721..64372232	hg38	UCSC Ensembl
Inner	chr15:64664135..64664227	hg19	UCSC Ensembl
Outer	chr15:64663920..64664431	hg19	UCSC Ensembl
Inner	chr15:62451188..62451280	hg18	UCSC Ensembl
Outer	chr15:62450973..62451484	hg18	UCSC Ensembl

Cytoband

15q22.31

Allele length

Assembly	Allele length
hg38	512
hg19	512
hg18	512

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2319425

Supporting Variants

Samples

NA18507

Known Genes

KIAA0101

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)

essv4691769

Frequency

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