Variant Details

Variant: esv2228566

Internal ID

7899677

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr3:15592555..15592995	hg38	UCSC Ensembl
Outer	chr3:15592490..15593048	hg38	UCSC Ensembl
Inner	chr3:15634062..15634502	hg19	UCSC Ensembl
Outer	chr3:15633997..15634555	hg19	UCSC Ensembl
Inner	chr3:15609066..15609506	hg18	UCSC Ensembl
Outer	chr3:15609001..15609559	hg18	UCSC Ensembl

Cytoband

3p24.3

Allele length

Assembly	Allele length
hg38	559
hg19	559
hg18	559

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4852750

Samples

NA18507

Known Genes

HACL1

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)

esv2228566

Frequency

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