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. 2021 Apr 26;21:386. doi: 10.1186/s12879-021-06076-w

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — Analysis of viral titer association with UL146 genotype, gender, and sample age. a Box-whisker plot of sample CMV titer and the UL146 genotype found in the sample. Non-ELR UL146 genotypes are marked in blue. No significant differences were found in a one-way ANOVA with Tukey’s multiple comparison test, n = 116. b Box-whisker plot of sample CMV titer and gender showing no association, n = 120. c Scatter plot of sample age and CMV titer with a linear regression line showing no significant correlation, n = 120. Non-ELR UL146 genotypes are marked in blue. d Congenital CMV diagnoses over the study period per birth year for a total of 451 registered cases