Fig. 3
From: Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia
CNVs within SYCE1 identified in the NOA-affected family using CNV array. A–C CNV array revealed the CNV (seq[GRCh37] del(10)(10q26.3)chr10:g.135111754_135427143del) in the proband (P6326) (A), father (B) and mother (C); D–F CNV array revealed the CNV (seq[GRCh37] del(10)(10q26.3)chr10:g.135340247_135379115del) in the NOA-affected patient (P10377) (D), father (E) and mother (F)