Variant Details

Variant: essv4934836

Internal ID

7520468

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr20:64178427..64179121	hg38	UCSC Ensembl
Outer	chr20:64178361..64179164	hg38	UCSC Ensembl
Inner	chr20:62809780..62810474	hg19	UCSC Ensembl
Outer	chr20:62809714..62810517	hg19	UCSC Ensembl
Inner	chr20:62280224..62280918	hg18	UCSC Ensembl
Outer	chr20:62280158..62280961	hg18	UCSC Ensembl

Cytoband

20q13.33

Allele length

Assembly	Allele length
hg38	804
hg19	804
hg18	804

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2097509

Supporting Variants

Samples

NA18507

Known Genes

MYT1

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)

essv4934836

Frequency

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