Variant Details

Variant: esv2067068

Internal ID

7738179

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr6:128655200..128655414	hg38	UCSC Ensembl
Outer	chr6:128655018..128655594	hg38	UCSC Ensembl
Inner	chr6:128976345..128976559	hg19	UCSC Ensembl
Outer	chr6:128976163..128976739	hg19	UCSC Ensembl
Inner	chr6:129018038..129018252	hg18	UCSC Ensembl
Outer	chr6:129017856..129018432	hg18	UCSC Ensembl

Cytoband

6q22.33

Allele length

Assembly	Allele length
hg38	577
hg19	577
hg18	577

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4925387

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)

esv2067068

Frequency

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