Variant Details

Variant: essv4938269

Internal ID

7523901

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:24638326..24638628	hg38	UCSC Ensembl
Outer	chr7:24638104..24638845	hg38	UCSC Ensembl
Inner	chr7:24677945..24678247	hg19	UCSC Ensembl
Outer	chr7:24677723..24678464	hg19	UCSC Ensembl
Inner	chr7:24644470..24644772	hg18	UCSC Ensembl
Outer	chr7:24644248..24644989	hg18	UCSC Ensembl

Cytoband

7p15.3

Allele length

Assembly	Allele length
hg38	742
hg19	742
hg18	742

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2168364

Supporting Variants

Samples

NA18507

Known Genes

MPP6

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)

essv4938269

Frequency

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