Skip to main content
. Author manuscript; available in PMC: 2022 Jun 1.
Published in final edited form as: Ophthalmic Genet. 2021 Mar 15;42(3):320–325. doi: 10.1080/13816810.2021.1888127

Figure 3.

Figure 3.

(a) Coverage and alignment tracks in the IGV browser. No read with the 20-bp deletion was found the parents’ data. Sequences of mismatched bases are shown. The reads with mismatched CGGCGGC are expected to contain the 20 nucleotides deletion due to misalignment because of the repeat in the reference sequence. (b) Previously reported predicted SOX2 protein familial variants.