De novo and inherited private variants in MAP1B in periventricular nodular heterotopia
Fig 2
Distribution of MAP1B LOF alleles in PVNH cases (red dots), in individuals from ExAC and gnomAD databases (blue dots with number of alleles observed represented by number of dots running vertically at this site), and in the Deciphering Developmental Disorders case (orange dot).
A Sanger confirmed de novo variant is indicated with a white dot in the circle.