Variant Details

Variant: essv4529276

Internal ID

7114908

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr20:10802740..10802812	hg38	UCSC Ensembl
Outer	chr20:10802545..10803013	hg38	UCSC Ensembl
Inner	chr20:10783388..10783460	hg19	UCSC Ensembl
Outer	chr20:10783193..10783661	hg19	UCSC Ensembl
Inner	chr20:10731388..10731460	hg18	UCSC Ensembl
Outer	chr20:10731193..10731661	hg18	UCSC Ensembl

Cytoband

20p12.2

Allele length

Assembly	Allele length
hg38	469
hg19	469
hg18	469

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2045561

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)

essv4529276

Frequency

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