Variant Details

Variant: essv4664565

Internal ID

7250197

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr20:23122669..23123004	hg38	UCSC Ensembl
Outer	chr20:23122511..23123145	hg38	UCSC Ensembl
Inner	chr20:23103306..23103641	hg19	UCSC Ensembl
Outer	chr20:23103148..23103782	hg19	UCSC Ensembl
Inner	chr20:23051306..23051641	hg18	UCSC Ensembl
Outer	chr20:23051148..23051782	hg18	UCSC Ensembl

Cytoband

20p11.21

Allele length

Assembly	Allele length
hg38	635
hg19	635
hg18	635

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv1954583

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)

essv4664565

Frequency

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