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. 2021 Nov 11;12:6501. doi: 10.1038/s41467-021-26856-x

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© The Author(s) 2021

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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Fig. 1 — a Studied sample information overview, “NA” denotes not available. b Distribution of the base-mapping rate of clean data aligned to the reference genome GRCh38. c Error rate represented as percentage for each type (n = 405 per group). d Average number of SVs identified by Sniffles, NanoVar and NanoSV per individual and the overlap among them. e Average number of SVs after each filtering step (n = 405 per group), “Original” represents unfiltered SVs detected by at least two callers, “Depth”, “Length”, and “Region” represent SVs filtered according to the supported read number, extra-long intervals, and very low-complexity regions, respectively. f Number of SVs of each type in each individual. Data are represented as mean ± SD in c and e.