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. 2023 Jan 19;29(1):180–189. doi: 10.1038/s41591-022-02142-1

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© Crown 2023, corrected publication 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 2 — A sunburst plot representing all 200 families separated by the type of pregnancy loss (2nd, most inner ring), across different organ systems (third ring), the genomic findings (fourth ring) and candidate disease genes (fifth, most outer ring). The genomic findings are separated by LP/P ((Likely) pathogenic), VUS (variant of uncertain significance), GUS (gene of uncertain significance), and NAD (no abnormalities detected). The percentages in the right-side legend represent the number of variants identified across the different pregnancy groups. This plot shows that the study cohort mostly consisted of termination of pregnancies. The input data for the sunburst plot was generated from Supplementary Table 2. All sunburst plots were generated using the sunburstR package (https://github.com/timelyportfolio/sunburstR).