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Table 6 CNVs associated with fragile site FRA16D and FRA3B

From: Expanding the genetic basis of copy number variation in familial breast cancer

Chr

Start (bp)

End (bp)

Size (Kb)

Gene

Probes

DGV

16

76,684,338

76,929,109

244.8

WWOX

222

Reported

16

76,947,909

77,009,160

61.3

WWOX

69

Reported

3

60,494,885

60,632,282

137.4

FHIT

158

 
  1. CNV location (chromosome, start bp and end bp) and size (Kb); as well as the confidence score associated with CNV call, the gene affected by the variant, the number of probes used to call the CNV and if the variant has previously been reported in the DGV.
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Hereditary Cancer in Clinical Practice

ISSN: 1897-4287