Variant Details

Variant: essv4858361

Internal ID

7443993

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr8:143014481..143014780	hg38	UCSC Ensembl
Outer	chr8:143014398..143014840	hg38	UCSC Ensembl
Inner	chr8:144095898..144096197	hg19	UCSC Ensembl
Outer	chr8:144095815..144096257	hg19	UCSC Ensembl
Inner	chr8:144167273..144167572	hg18	UCSC Ensembl
Outer	chr8:144167190..144167632	hg18	UCSC Ensembl

Cytoband

8q24.3

Allele length

Assembly	Allele length
hg38	443
hg19	443
hg18	443

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2204670

Supporting Variants

Samples

NA18507

Known Genes

LOC100133669

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)

essv4858361

Frequency

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