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Table 1 Deep sequencing of the family members in mosaic DMD cases

From: Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report

Sample Name Mutant sites
ChrX-31,947,831 (c.6794delG) ChrX-31,947,829 (c.6796delA)
Depth Frequency (%) Result Depth Frequency (%) Result
Proband 522/568 91.90 Hemi 2/569 0.0 Non-carrier
Mother carrier
(Pregnancy)
164/463 35.32 Het 18/465 3.87 Low level
mosaicism
Amniotic Fluid 26/1435 0.0 Non-carrier 656/1446 45.36 Het
Mother carrier
(Non-pregnancy)
517/1229 42.07 Het 65/1224 5.31 Low level
mosaicism