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. 2020 Apr 15;11:614. doi: 10.3389/fimmu.2020.00614

Figure 2.

Figure 2

Flow chart describing the numbers of variants identified by GSA array compared to conventional methods in 95 clinically diagnosed PID patients in the first run. CNV, copy number variants; DCLRE1C: GSA, Global Screening Array; PCR, Sanger sequencing; NGS, next-sequencing sequence; PID, Primary immunodeficiency disorder; SNV, single nucleotide variants.