Skip to main content
Fig. 2 | BMC Medical Genomics

Fig. 2

From: Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia

Fig. 2

WES and Sanger sequencing of SYCE1 SNV in the NOA-affected patient. A Blood samples from the NOA-affected patient and his parents were detected with WES. Frameshift variant (F230fs) was identified in the proband and his father. The maternal allele appears to be normal. BD Validation of SYCE1 SNV identified in WES using Sanger sequencing in the patient (P6326) (B) and his parents (C and D)

Back to article page