Variant Details

Variant: essv4522195

Internal ID

6761141

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr4:169229941..169230092	hg38	UCSC Ensembl
Outer	chr4:169229774..169230251	hg38	UCSC Ensembl
Inner	chr4:170151092..170151243	hg19	UCSC Ensembl
Outer	chr4:170150925..170151402	hg19	UCSC Ensembl
Inner	chr4:170387667..170387818	hg18	UCSC Ensembl
Outer	chr4:170387500..170387977	hg18	UCSC Ensembl

Cytoband

4q32.3

Allele length

Assembly	Allele length
hg38	478
hg19	478
hg18	478

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv1943131

Supporting Variants

Samples

NA18507

Known Genes

SH3RF1

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)

essv4522195

Frequency

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