Variant Details

Variant: essv4815649

Internal ID

7401281

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr5:109259389..109265419	hg38	UCSC Ensembl
Outer	chr5:109259197..109265623	hg38	UCSC Ensembl
Inner	chr5:108595090..108601120	hg19	UCSC Ensembl
Outer	chr5:108594898..108601324	hg19	UCSC Ensembl
Inner	chr5:108622989..108629019	hg18	UCSC Ensembl
Outer	chr5:108622797..108629223	hg18	UCSC Ensembl

Cytoband

5q21.3

Allele length

Assembly	Allele length
hg38	6427
hg19	6427
hg18	6427

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2305572

Supporting Variants

Samples

NA18507

Known Genes

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)

essv4815649

Frequency

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