Variant Details

Variant: essv4939271

Internal ID

7178217

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr4:24964834..24965509	hg38	UCSC Ensembl
Outer	chr4:24964653..24965706	hg38	UCSC Ensembl
Inner	chr4:24966456..24967131	hg19	UCSC Ensembl
Outer	chr4:24966275..24967328	hg19	UCSC Ensembl
Inner	chr4:24575554..24576229	hg18	UCSC Ensembl
Outer	chr4:24575373..24576426	hg18	UCSC Ensembl

Cytoband

4p15.2

Allele length

Assembly	Allele length
hg38	1054
hg19	1054
hg18	1054

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2023485

Supporting Variants

Samples

NA18507

Known Genes

CCDC149

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)

essv4939271

Frequency

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