Variant Details

Variant: nsv826979

Internal ID

16089453

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr14:73534747..73546713	hg38	UCSC Ensembl
Inner	chr14:74001451..74013417	hg19	UCSC Ensembl
Inner	chr14:73071204..73083170	hg18	UCSC Ensembl

Cytoband

14q24.3

Allele length

Assembly	Allele length
hg38	11967
hg19	11967
hg18	11967

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

nssv1440644, nssv1429392, nssv1429939, nssv1439265, nssv1435400, nssv1422932, nssv1436162, nssv1433972, nssv1435885, nssv1441475, nssv1438437, nssv1431622, nssv1437011

Samples

NA18947, NA18592, NA18526, NA18969, NA18942, NA18973, NA18951, NA18566, NA18542, NA18564, AK18, AK12, NA18552

Known Genes

ACOT1, HEATR4

Method

Oligo aCGH

Analysis

To select parameters for calling CNVs (that is, the statistical threshold of the ADM2 algorithm, the minimum +/- log2 ratio and the minimum number of consecutive probes in a CNV interval), we calculated the sensitivity and positive predictive value based on the comparison of aCGH-based CNV calls (using our high-resolution Agilent 24M platform) with read-depth sequence data for two samples from Korean individuals (AK1 and AK2). We attempted to obtain `absolute' copy number status of the sample from NA10851, which was used as the reference sample for aCGH experiments in this study. For this, we used read-depth data for NA10851 obtained from massively parallel sequencing by the Illumina GA II data. The read-depth data represent the copy number status of NA10851 as compared to the human reference genome (hg18) because the short read sequences were aligned to hg18.

Platform

Agilent 24M aCGH

Comments

Reference

Park_et_al_2010

Pubmed ID

20364138

Accession Number(s)

nsv826979

Frequency

Sample Size	31
Observed Gain	0
Observed Loss	13
Observed Complex	0
Frequency	n/a